Variant report

Variant	nsv436477
Chromosome Location	chr5:59946381-59952080
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:76)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:76 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:59948213-59948360	K562	blood:	n/a	n/a
2	CBX3	chr5:59949056-59949287	K562	blood:	n/a	n/a
3	CEBPB	chr5:59947408-59947609	HepG2	liver:	n/a	n/a
4	CEBPB	chr5:59947819-59948439	MCF-7	breast:	n/a	chr5:59948192-59948203
5	CEBPB	chr5:59948060-59948362	HepG2	liver:	n/a	chr5:59948192-59948203
6	CEBPB	chr5:59947859-59948500	A549	lung:	n/a	chr5:59948192-59948203
7	CEBPB	chr5:59948006-59948383	A549	lung:	n/a	chr5:59948192-59948203
8	CEBPB	chr5:59947835-59948505	MCF-7	breast:	n/a	chr5:59948192-59948203
9	CEBPB	chr5:59947984-59948374	K562	blood:	n/a	chr5:59948192-59948203
10	CEBPB	chr5:59947390-59948442	IMR90	lung:	n/a	chr5:59948192-59948203
11	CEBPB	chr5:59947986-59948470	HCT-116	colon:	n/a	chr5:59948192-59948203
12	CEBPB	chr5:59947994-59948374	K562	blood:	n/a	chr5:59948192-59948203
13	CEBPB	chr5:59948015-59948330	K562	blood:	n/a	chr5:59948192-59948203
14	CEBPB	chr5:59947973-59948387	A549	lung:	n/a	chr5:59948192-59948203
15	CEBPB	chr5:59948016-59948391	Hela-S3	cervix:	n/a	chr5:59948192-59948203
16	CTCF	chr5:59948020-59948170	HBMEC	blood vessel:	n/a	n/a
17	CTCF	chr5:59948980-59949130	NHDF-neo	bronchial:	n/a	n/a
18	CTCF	chr5:59949060-59949210	NHDF-neo	bronchial:	n/a	n/a
19	EP300	chr5:59948192-59948358	K562	blood:	n/a	n/a
20	FOS	chr5:59948060-59948458	MCF10A-Er-Src	breast:	n/a	chr5:59948263-59948274
21	FOS	chr5:59948042-59948459	MCF10A-Er-Src	breast:	n/a	chr5:59948263-59948274
22	FOS	chr5:59948026-59948483	MCF10A-Er-Src	breast:	n/a	chr5:59948263-59948274
23	FOS	chr5:59948038-59948450	MCF10A-Er-Src	breast:	n/a	chr5:59948263-59948274
24	FOS	chr5:59948040-59948472	HUVEC	blood vessel:	n/a	chr5:59948263-59948274
25	FOSL1	chr5:59948005-59948477	HCT-116	colon:	n/a	n/a
26	FOSL2	chr5:59947962-59948478	MCF-7	breast:	n/a	n/a
27	FOSL2	chr5:59948004-59948479	A549	lung:	n/a	n/a
28	FOSL2	chr5:59948083-59948390	A549	lung:	n/a	n/a
29	FOSL2	chr5:59947940-59948567	SK-N-SH	brain:	n/a	n/a
30	FOSL2	chr5:59947971-59948512	MCF-7	breast:	n/a	n/a
31	GATA3	chr5:59947934-59948451	SK-N-SH	brain:	n/a	n/a
32	GTF2F1	chr5:59949203-59949232	H1-hESC	embryonic stem cell:	n/a	n/a
33	IRF1	chr5:59948146-59948381	K562	blood:	n/a	n/a
34	JUN	chr5:59948067-59948423	Hela-S3	cervix:	n/a	n/a
35	JUN	chr5:59948084-59948421	K562	blood:	n/a	n/a
36	JUN	chr5:59947935-59948476	K562	blood:	n/a	n/a
37	JUND	chr5:59947887-59948606	SK-N-SH	brain:	n/a	chr5:59948263-59948274
38	JUND	chr5:59948102-59948403	HepG2	liver:	n/a	chr5:59948263-59948274
39	JUND	chr5:59948013-59948454	K562	blood:	n/a	chr5:59948263-59948274
40	JUND	chr5:59947923-59948557	SK-N-SH	brain:	n/a	chr5:59948263-59948274
41	JUND	chr5:59948065-59948455	Hela-S3	cervix:	n/a	chr5:59948263-59948274
42	JUND	chr5:59947932-59948469	SK-N-SH	brain:	n/a	chr5:59948263-59948274
43	MAFF	chr5:59948102-59948392	K562	blood:	n/a	n/a
44	MAFK	chr5:59947808-59947873	HepG2	liver:	n/a	n/a
45	MAFK	chr5:59948111-59948404	K562	blood:	n/a	n/a
46	MAFK	chr5:59947791-59948401	IMR90	lung:	n/a	n/a
47	MYC	chr5:59948090-59948352	MCF10A-Er-Src	breast:	n/a	n/a
48	MYC	chr5:59948081-59948402	MCF10A-Er-Src	breast:	n/a	n/a
49	NFYB	chr5:59948105-59948351	Hela-S3	cervix:	n/a	n/a
50	PBX3	chr5:59947939-59948447	SK-N-SH	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:59947488-59947538	SK-N-SH_RA	brain:	n/a
2	chr5:59947488-59947538	HMEC	breast:	n/a
3	chr5:59947488-59947538	AG04449	skin:	fetal
4	chr5:59947488-59947538	RPTEC	kidney:	n/a
5	chr5:59947488-59947538	HCT-116	colon:	n/a
6	chr5:59947488-59947538	HUVEC	blood vessel:	n/a
7	chr5:59947488-59947538	IMR90	lung:	fetal
8	chr5:59947488-59947538	Caco-2	colon:	n/a
9	chr5:59947488-59947538	NB4	blood:	n/a
10	chr5:59947488-59947538	U87	brain:	n/a
11	chr5:59947488-59947538	HEK293	kidney:	embryo
12	chr5:59947488-59947538	GM12891	blood:	n/a
13	chr5:59947488-59947538	T-47D	breast:	n/a
14	chr5:59947488-59947538	SK-N-MC	brain:	n/a
15	chr5:59947488-59947538	HCPEpiC	choroid plexus:	n/a
16	chr5:59947488-59947538	HCM	heart:	n/a
17	chr5:59947488-59947538	HIPEpiC	eye:	n/a
18	chr5:59947488-59947538	GM12892	blood:	n/a
19	chr5:59947488-59947538	H1-hESC	embryonic stem cell:	embryo
20	chr5:59947488-59947538	PFSK-1	brain:	n/a
21	chr5:59947488-59947538	BJ	skin:	n/a
22	chr5:59947488-59947538	AG09309	skin:	n/a
23	chr5:59947488-59947538	AG10803	skin:	n/a
24	chr5:59947488-59947538	AG04450	lung:	fetal
25	chr5:59947488-59947538	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:59947488-59947538	NHDF-neo	bronchial:	n/a
27	chr5:59947488-59947538	MCF10A-Er-Src	breast:	n/a
28	chr5:59947488-59947538	ECC-1	luminal epithelium:	n/a
29	chr5:59947488-59947538	HEEpiC	esophagus:	n/a
30	chr5:59947488-59947538	NT2-D1	testis:	n/a
31	chr5:59947488-59947538	GM19239	blood:	n/a
32	chr5:59947488-59947538	HRCEpiC	kidney:	n/a
33	chr5:59947488-59947538	PANC-1	pancreas:	n/a
34	chr5:59947488-59947538	ProgFib	skin:	n/a
35	chr5:59947488-59947538	ovcar-3	ovarian:	n/a
36	chr5:59947488-59947538	CMK	blood:	n/a
37	chr5:59947488-59947538	HCF	heart:	n/a
38	chr5:59947488-59947538	SAEC	small airway:	n/a
39	chr5:59947488-59947538	Hepatocyte	liver:	n/a
40	chr5:59947488-59947538	Hela-S3	cervix:	n/a
41	chr5:59947488-59947538	BE2_C	brain:	n/a
42	chr5:59947488-59947538	GM12878	blood:	n/a
43	chr5:59947488-59947538	SKMC	muscle:	n/a
44	chr5:59947488-59947538	K562	blood:	n/a
45	chr5:59947488-59947538	HNPCEpiC	eye:	n/a
46	chr5:59947488-59947538	HAEpiC	amniotic membrane:	n/a
47	chr5:59947488-59947538	NHBE	bronchial:	n/a
48	chr5:59947488-59947538	MCF-7	breast:	n/a
49	chr5:59947488-59947538	NH-A	brain:	n/a
50	chr5:59947488-59947538	PrEC	prostate:	n/a

(count:1 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:59942675..59945605-chr5:59945905..59947831,2	K562	blood:

No data

Variant related genes	Relation type
DEPDC1B	TF binding region
DEPDC1B	CpG island
ENSG00000035499	chromatin interactions

Extended variants
information (count: 189 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:189 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535211245	chr5:59946440-59946441	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs181012673	chr5:59946479-59946480	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs76705107	chr5:59946481-59946482	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs550908551	chr5:59946530-59946531	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs367679950	chr5:59946531-59946532	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs79988462	chr5:59946534-59946535	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs74785192	chr5:59946560-59946561	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs576272902	chr5:59946592-59946593	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs545320081	chr5:59946596-59946597	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs542409068	chr5:59946657-59946658	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs565010935	chr5:59946731-59946732	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs572250996	chr5:59946850-59946851	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs114567370	chr5:59946884-59946885	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs139508506	chr5:59947078-59947079	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs144182021	chr5:59947183-59947184	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs371673471	chr5:59947212-59947213	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs530089409	chr5:59947238-59947239	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs549786356	chr5:59947248-59947249	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs373845683	chr5:59947279-59947280	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs528904505	chr5:59947286-59947287	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs563667152	chr5:59947287-59947288	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs532388389	chr5:59947304-59947305	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs2045356	chr5:59947354-59947355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs35534827	chr5:59947356-59947357	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs374227777	chr5:59947360-59947361	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs200301371	chr5:59947366-59947367	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs374196686	chr5:59947367-59947368	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs3029124	chr5:59947376-59947377	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs372737443	chr5:59947386-59947387	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs150616364	chr5:59947414-59947415	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs567387927	chr5:59947458-59947459	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs536315622	chr5:59947485-59947486	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs184204557	chr5:59947488-59947489	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs139181008	chr5:59947522-59947523	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs538251677	chr5:59947563-59947564	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs189528331	chr5:59947577-59947578	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs34002879	chr5:59947609-59947610	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs543307324	chr5:59947623-59947624	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs571969674	chr5:59947627-59947628	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs116030463	chr5:59947633-59947634	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs560722205	chr5:59947679-59947680	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs574609268	chr5:59947730-59947731	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs543546429	chr5:59947745-59947746	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs533305539	chr5:59947764-59947765	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs370083487	chr5:59947902-59947903	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs563611147	chr5:59947940-59947941	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs181801437	chr5:59947971-59947972	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs552281811	chr5:59947995-59947996	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs186115822	chr5:59948012-59948013	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs149965805	chr5:59948030-59948031	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Bipolar disorder	19114987	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59920600-59947800	Weak transcription	HUVEC	blood vessel
2	chr5:59925200-59947200	Weak transcription	Pancreas	Pancrea
3	chr5:59926400-59967800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr5:59929400-59947400	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr5:59929400-59954600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr5:59929600-59948000	Weak transcription	NHEK	skin
7	chr5:59933400-59965200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr5:59933600-59981000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr5:59934800-59947600	Weak transcription	HMEC	breast
10	chr5:59936600-59961400	Weak transcription	Thymus	Thymus
11	chr5:59936800-59961800	Weak transcription	Fetal Thymus	thymus
12	chr5:59940400-59947800	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr5:59940400-59947800	Weak transcription	HSMM	muscle
14	chr5:59940600-59947400	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr5:59940600-59947600	Weak transcription	A549	lung
16	chr5:59940600-59948000	Weak transcription	K562	blood
17	chr5:59940600-59950200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr5:59941000-59947200	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr5:59941200-59946600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr5:59941200-59947600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr5:59942600-59947400	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr5:59942800-59952000	Weak transcription	Dnd41	blood
23	chr5:59942800-59961600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr5:59943400-59947600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr5:59943400-59947800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr5:59943400-59952400	Weak transcription	Placenta	Placenta
27	chr5:59943400-59977000	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr5:59943800-59952600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr5:59944400-59952400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr5:59945000-59961800	Weak transcription	HepG2	liver
31	chr5:59946200-59946400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:59946400-59952400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr5:59946800-59947800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr5:59947000-59947800	Enhancers	NHLF	lung
35	chr5:59947200-59948600	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr5:59947400-59947800	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr5:59947400-59947800	Enhancers	NH-A	brain
38	chr5:59947400-59947800	Enhancers	NHDF-Ad	bronchial
39	chr5:59947400-59947800	Enhancers	Osteobl	bone
40	chr5:59947400-59948400	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr5:59947400-59948800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr5:59947400-59949000	Enhancers	Muscle Satellite Cultured Cells	--
43	chr5:59947600-59947800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr5:59947600-59947800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr5:59947600-59948200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr5:59947600-59948200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr5:59947600-59948200	Enhancers	Placenta Amnion	Placenta Amnion
48	chr5:59947600-59948200	ZNF genes & repeats	A549	lung
49	chr5:59947600-59948200	Enhancers	HMEC	breast
50	chr5:59947600-59948600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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